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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:0080872 | primary ovarian insufficiency 15 | HGNC:23168 | Homo sapiens (human) | 57697 | FANCM |
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| DOID:0112381 | muscular dystrophy-dystroglycanopathy type C12 | HGNC:26267 | Homo sapiens (human) | 84197 | POMK |
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| DOID:0110509 | autosomal recessive nonsyndromic deafness 53 | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0060645 | chronic recurrent multifocal osteomyelitis | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:0111345 | transient bullous dermolysis of the newborn | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:0111235 | congenital muscular dystrophy-dystroglycanopathy type A12 | HGNC:26267 | Homo sapiens (human) | 84197 | POMK |
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| DOID:1612 | breast cancer | HGNC:9277 | Homo sapiens (human) | 8493 | PPM1D |
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| DOID:0050419 | complement factor I deficiency | HGNC:5394 | Homo sapiens (human) | 3426 | CFI |
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| DOID:5419 | schizophrenia | HGNC:18601 | Homo sapiens (human) | 65078 | RTN4R |
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| DOID:0050534 | congenital stationary night blindness | HGNC:4689 | Homo sapiens (human) | 3000 | GUCY2D |
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| DOID:0110734 | neurodegeneration with brain iron accumulation | HGNC:3976 | Homo sapiens (human) | 2495 | FTH1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:8086 | Homo sapiens (human) | 4938 | OAS1 |
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| DOID:0050733 | methylmalonic aciduria and homocystinuria type cblG | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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| DOID:13564 | aspergillosis | HGNC:14558 | Homo sapiens (human) | 64581 | CLEC7A |
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| DOID:0070490 | infantile parkinsonism-dystonia 2 | HGNC:10935 | Homo sapiens (human) | 6571 | SLC18A2 |
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| DOID:0081331 | glycogen storage disease Ic | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:14735 | hereditary angioedema | HGNC:14178 | Homo sapiens (human) | 64711 | HS3ST6 |
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| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:18358 | Homo sapiens (human) | 84818 | IL17RC |
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| DOID:0070031 | autosomal dominant intellectual developmental disorder 1 | HGNC:20444 | Homo sapiens (human) | 55777 | MBD5 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:3765 | Homo sapiens (human) | 2322 | FLT3 |
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| DOID:0080429 | developmental and epileptic encephalopathy 24 | HGNC:4845 | Homo sapiens (human) | 348980 | HCN1 |
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| DOID:0080718 | GNE myopathy | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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| DOID:0110383 | retinitis pigmentosa 7 | HGNC:10254 | Homo sapiens (human) | 6094 | ROM1 |
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| DOID:0110057 | amelogenesis imperfecta type 2A1 | HGNC:6365 | Homo sapiens (human) | 9622 | KLK4 |
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| DOID:10534 | stomach cancer | HGNC:3430 | Homo sapiens (human) | 2064 | ERBB2 |
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